34142 Federal Register / Vol. 70, No.
112 / Monday, June 13, 2005 / Notices
Approved but Unfunded Applications
Applications that are approved but
unfunded may be held over for funding
in the next funding cycle, pending the
availability of funds, for a period not to
exceed one year.
3. Anticipated Announcement and
Award Dates
Applications will be reviewed during
the Summer 2005. Grant awards will
have a start date no later than
September 30, 2005.
VI. Award Administration Information
1. Award Notices
The successful applicants will be
notified through the issuance of a
Financial Assistance Award document
which sets forth the amount of funds
granted, the terms and conditions of the
grant, the effective date of the grant, the
budget period for which initial support
will be given, the non-Federal share to
be provided, and the total project period
for which support is contemplated. The
Financial Assistance Award will be
signed by the Grants Officer and
transmitted via postal mail.
Organizations whose applications will
not be funded will be notified in
writing.
2. Administrative and National Policy
Requirements
Grantees are subject to the
requirements in 45 CFR part 74 (non-
governmental) or 45 CFR part 92
(governmental).
Direct Federal grants, sub-award
funds, or contracts under this program
shall not be used to support inherently
religious activities such as religious
instruction, worship, or proselytization.
Therefore, organizations must take steps
to separate, in time or location, their
inherently religious activities from the
services funded under this program.
Regulations pertaining to the
prohibition of Federal funds for
inherently religious activities can be
found on the HHS Web site at http://
www.os.dhhs.gov/fbci/waisgate21.pdf.
3. Reporting Requirements
Program Progress Reports: Semi-
Annually.
Financial Reports: Semi-Annually.
Grantees will be required to submit
program progress and financial reports
(SF 269) throughout the project period.
Program progress and financial reports
are due 30 days after the reporting
period. In addition, final programmatic
and financial reports are due 90 days
after the close of the project period.
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VII. Agency Contacts
Program Office Contact: Pat
Campiglia, Children’s Bureau, 330 C
Street, SW., Washington, DC 20447,
Phone: (202) 205–8060, e-mail:
pcampiglia@acf.hhs.gov.
Grants Management Office Contact:
Peter Thompson, Grants Officer,
Administration for Children and
Families, Children’s Bureau, 330 C
Street, SW. Room 2070, Washington, DC
20447, Phone: (202) 401–4608, e-mail:
pathompson@acf.hhs.gov.
VIII. Other Information
Additional information about this
program and its purpose can be located
on the following Web sites: http://
www.acf.hhs.gov/programs/cb/.
For general information regarding this
announcement please contact: ACYF
Operations Center, c/o The Dixon
Group, Inc. Attn: Children’s Bureau, 118
Q St., NE., Washington, DC 20002–2132,
Telephone: 866–796–1591.
Notice: Beginning with FY 2005, the
Administration for Children and
Families (ACF) will no longer publish
grant announcements in the Federal
Register. Beginning October 1, 2005,
applicants will be able to find a
synopsis of all ACF grant opportunities
and apply electronically for
opportunities via: http://
www.Grants.gov. Applicants will also be
able to find the complete text of
http://www.acf.hhs.gov/grants/
index.html.
Please reference Section IV.3 for
details about acknowledgement of
received applications.
Dated: June 2, 2005.
Joan E. Ohl,
Commissioner, Administration on Children,
Youth, and Families.
[FR Doc. 05–11592 Filed 6–10–05; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Correction
The Office of Community Services
Program Announcement HHS–2005–
ACF–OCS–EN–0018 was published in
the Federal Register on June 6, 2005.
On page 32794 of this announcement,
the due date for applications is July 21,
2005.
On page 32800 of this announcement,
the due date for applications is August
5, 2005.
The correct due date for applications
for this announcement is July 21, 2005.
PO 00000 Frm 00061 Fmt 4703 Sfmt 4703 E:\FR\FM\13JNN1.SGM
Dated: June 6, 2005.
Josephine B. Robinson,
Director, Office of Community Services.
[FR Doc. 05–11591 Filed 6–10–05; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2005N–0217]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Cosmetic Product
Voluntary Reporting Program
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the collection of information associated
with the Cosmetic Product Voluntary
Reporting Program.
DATES: Submit written or electronic
comments on the collection of
information by August 12, 2005.
ADDRESSES: Submit electronic
comments on the collection of
information to: http://www.fda.gov/
dockets/ecomments. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Peggy Robbins, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–1223.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
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 Federal Register / Vol. 70, No. 112 / Monday, June 13, 2005 / Notices
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
21 CFR Section Form No.
720.1 through FDA 2512 and
720.4 (new sub- FDA 2512a
missions)
720.4 and 720.6 FDA 2512 and
(amendments) FDA 2512a
720.3 and 720.6 FDA 2514
(notices of dis-
continuance)
720.8 (requests for
confidentiality)
Total
1 There are no capital costs or operating and maintenance costs associated with this collection of information.
VerDate jul<14>2003 16:45 Jun 10, 2005 Jkt 205001
Cosmetic Product Voluntary Reporting
Program—21 CFR Part 720 (OMB
Control Number 0910–0030)—Extension
Under the Federal Food, Drug, and
Cosmetic Act (the act), cosmetic
products that are adulterated under
section 601 of the act (21 U.S.C. 361),
or misbranded under section 602 of the
act (21 U.S.C. 362), cannot legally be
distributed in interstate commerce. To
assist FDA in carrying out its
responsibility to regulate cosmetics,
FDA requests under part 720 (21 CFR
part 720), but does not require, that
firms that manufacture, pack, or
distribute cosmetics file with the agency
an ingredient statement for each of their
products. Ingredient statements for new
submissions (§§ 720.1 through 720.4)
are reported on Form FDA 2512,
‘‘Cosmetic Product Ingredient
Statement,’’ and on Form FDA 2512a, a
continuation form. Amendments to
product formulations (§§ 720.3, 720.4,
and 720.6) also are reported on Forms
FDA 2512 and FDA 2512a. When a firm
discontinues the commercial
distribution of a cosmetic, FDA requests
that the firm file Form FDA 2514,
‘‘Discontinuance of Commercial
Distribution of Cosmetic Product
Formulation’’ (§§ 720.3 and 720.6). If
any of the information submitted on or
with these forms is confidential, the
firm may submit a request for
confidentiality under § 720.8.
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
Annual Frequency
No. of Respondents
per Response
112 12.9
112 0.5
112 1 4
1 1
PO 00000 Frm 00062 Fmt 4703 Sfmt 4703 E:\FR\FM\13JNN1.SGM
34143
FDA places cosmetic product filing
information in a computer database and
uses the information for evaluation of
cosmetic products currently on the
market. Because filing of cosmetic
product formulations is not mandatory,
voluntary filings provide FDA with the
best information available about
cosmetic product ingredients and their
frequency of use, businesses engaged in
the manufacture and distribution of
cosmetics, and approximate rates of
product discontinuance and formula
modifications. The information assists
FDA scientists in evaluating reports of
alleged injuries and adverse reactions
from the use of cosmetics. The
information also is used in defining and
planning analytical and toxicological
studies pertaining to cosmetics.
Information from the database is
releasable to the public under FDA
compliance with the Freedom of
Information Act. FDA shares
nonconfidential information from its
files on cosmetics with consumers,
medical professionals, and industry.
FDA has developed an electronic
submission system for filing Forms FDA
2512, FDA 2512a, and FDA 2514 that
will reduce the reporting burden for
respondents and FDA. The system is
currently undergoing additional beta
testing and implementation is
anticipated for summer 2005.
FDA estimates the annual burden of
this collection of information as follows:
Total Annual Hours per Re-
Total Hours
Responses sponse
1,446 0.5 723
52 0.33 17
0.1 0.4
1 1.5 1.5
742
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 34144 Federal Register / Vol. 70, No. 112 / Monday, June 13, 2005 / Notices
These estimates are based on FDA’s
experience with the Cosmetic Product
Voluntary Reporting Program. The
estimated annual total hour burden is 75
percent of the burden reported in 2002
due to decreased submissions. However,
the number of respondents doubled, and
FDA attributes this to increased interest
in the program. FDA expects the
number of submissions to increase
accordingly in the next 3 years.
Dated: June 6, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05–11641 Filed 6–10–05; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Office for Women’s Services; Notice of
a Meeting
Pursuant to Pub. L. 92–463, notice is
hereby given of a Substance Abuse and
Mental Health Services
Administration’s (SAMHSA) Advisory
Committee for Women’s Services
teleconference meeting on June 21,
2005.
The meeting will be open and include
discussions on SAMHSA’s women’s
issues as they relate to the Agency’s
priority matrix. The meeting will also
include discussions on the Agency’s
current administrative, legislative and
policy developments.
Attendance by the public will be
limited to space available. Public
comments are welcome. Please
communicate with the individual listed
as contact below to make arrangements
to comment or to request special
accommodations for persons with
disabilities.
Substantive program information and
a roster of Committee members may be
obtained by accessing the SAMHSA
Advisory Council’s Web site (http://
www.samhsa.gov) as soon as possible
after the meeting or by communicating
with the contact whose name and
telephone number are listed below. The
transcript for the session will also be
available on the SAMHSA Advisory
Council Web site as soon as possible
after the meeting.
Committee Name: Substance Abuse and
Mental Health Services Administration
Advisory Committee for Women’s Services.
Meeting Date: June 21, 2005, 1 p.m.–3 p.m.
Place: 1 Choke Cherry Road, Conference
Room 8–1082, Rockville, MD 20857.
Type: Open.
Contact: Carol Watkins, Executive
Secretary, Advisory Committee for Women’s
VerDate jul<14>2003 16:45 Jun 10, 2005 Jkt 205001
Services, 1 Choke Cherry Road, Room 8–
1002, Rockville, MD 20857, Telephone: (240)
276–2254, Fax: (240) 276–2252, E-mail:
carol.watkin2@samhsa.gov.
Dated: June 6, 2005.
Toian Vaughn,
Committee Management Officer, Substance
Abuse and Mental Health Services
Administration.
[FR Doc. 05–11618 Filed 6–10–05; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HOMELAND
SECURITY
Coast Guard
[USCG–2005–21399]
Towing Safety Advisory Committee
AGENCY: Coast Guard, DHS.
ACTION: Notice of meetings.
SUMMARY: The Towing Vessel Inspection
Working Group of the Towing Safety
Advisory Committee (TSAC) will meet
to discuss matters relating to those
specific issues of towing safety. The
meetings will be open to the public.
DATES: The Towing Vessel Inspection
Working Group will meet on
Wednesday, June 22, 2005 from 1:30
p.m. to 4:30 p.m. and on Thursday, June
23, 2005 from 8:30 a.m. to 2 p.m. The
meetings may close early if all business
is finished. Written material and
requests to make oral presentations
should reach the Coast Guard on or
before June 15, 2005. Requests to have
a copy of your material distributed to
each member of the Working Group
should reach the Coast Guard on or
before June 15, 2005.
ADDRESSES: The Working Group will
meet at George Mason University,
Arlington Campus, 3301 Fairfax Drive,
Arlington, VA 22201. Please bring a
government-issued ID with photo (e.g.,
driver’s license). Send written material
and requests to make oral presentations
to Mr. Gerald Miante, Commandant (G-
MSO–1), U.S. Coast Guard
Headquarters, 2100 Second Street SW.,
Washington, DC 20593–0001. This
notice and related documents are
available on the Internet at http://
dms.dot.gov under the docket number
USCG–2004–21399.
FOR FURTHER INFORMATION CONTACT: Mr.
Gerald Miante, Assistant Executive
Director of TSAC, telephone 202–267–
0214, fax 202–267–4570, or e-mail
gmiante@comdt.uscg.mil.
SUPPLEMENTARY INFORMATION: Notice of
these meetings is given under the
Federal Advisory Committee Act, 5
PO 00000 Frm 00063 Fmt 4703 Sfmt 4703 E:\FR\FM\13JNN1.SGM
U.S.C. App. 2 (Pub. L. 92–463, 86 Stat.
770, as amended).
Agenda of Working Group Meetings:
The agenda for the Towing Vessel
Inspection Working Group tentatively
includes the following items:
(1) What proposed equipment
standards should be included in a
subchapter devoted to the inspection for
certification of towing vessels; and
(2) Which standards found in existing
regulations, if any, are suitable for
inclusion in a subchapter devoted to the
inspection for certification of towing
vessels?
Procedural
The meetings are open to the public.
Please note that the meetings may close
early if all business is finished. At the
Chair’s discretion, members of the
public may make oral presentations
during the meeting. If you would like to
make an oral presentation at the
meeting, please notify the Assistant
Executive Director (as provided above in
for further information contact) no later
than June 15, 2005. Written material for
distribution at the meeting should reach
the Coast Guard no later than June 15,
2005.
Information on Services for Individuals
With Disabilities
For information on facilities or
services for individuals with disabilities
or to request special assistance at the
meeting, contact Mr. Miante at the
number listed in FOR FURTHER
INFORMATION CONTACT as soon as
possible.
Dated: June 3, 2005.
Raymond Petow,
Acting Director of Standards, Marine Safety,
Security and Environmental Protection.
[FR Doc. 05–11588 Filed 6–10–05; 8:45 am]
BILLING CODE 4910–15–P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
North Mississippi National Wildlife
Refuge Complex
AGENCY: Fish and Wildlife Service,
Department of the Interior.
ACTION: Notice of Availability of the
Draft Comprehensive Conservation Plan
and Environmental Assessment for the
North Mississippi National Wildlife
Refuge Complex, which consists of three
national wildlife refuges—Coldwater
River, Dahomey, and Tallahatchie, as
well as a number of Farmers Home
Administration tracts in the northern
section of the Mississippi Delta.
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